Transporters in the kidney:
1: SLC22A3 solute carrier family 22 (extraneuronal monoamine transporter), member 3 [Homo sapiens]Other Aliases: HGNC:10967, EMT, EMTH, OCT3Other Designations: EMT organic cation transporter 3; extraneuronal monoamine transporter; organic cation transporter 3; solute carrier family 22 member 3Chromosome: 6; Location: 6q26-q27GeneID: 6581 2: SLC6A20 solute carrier family 6 (neurotransmitter transporter), member 20 [Homo sapiens]Other Aliases: HGNC:30927, XT3, Xtrp3Other Designations: X transporter protein 3; neurotransmitter transporter RB21A; orphan transporter XT3Chromosome: 3; Location: 3p21.3GeneID: 54716 3: SLC22A5 solute carrier family 22 (organic cation transporter), member 5 [Homo sapiens]Other Aliases: HGNC:10969, OCTN2Other Designations: high-affinity sodium dependent carnitine cotransporter; organic cation transporter 5; organic cation/carnitine transporter 2; solute carrier family 22 member 5Chromosome: 5; Location: 5q31GeneID: 6584 4: SLC22A6 solute carrier family 22 (organic anion transporter), member 6 [Homo sapiens]Other Aliases: HGNC:10970, HOAT1, MGC45260, OAT1, PAHT, ROAT1Other Designations: para-aminohippurate transporter; renal organic anion transporter 1; solute carrier family 22 member 6Chromosome: 11; Location: 11q13.1-q13.2GeneID: 9356 5: SLC22A7 solute carrier family 22 (organic anion transporter), member 7 [Homo sapiens]Other Aliases: HGNC:10971, MGC24091, MGC45202, NLT, OAT2Other Designations: liver-specific transporter; organic anion transporter 2; solute carrier family 22 member 7Chromosome: 6; Location: 6p21.2-p21.1GeneID: 10864 6: SLC22A12 solute carrier family 22 (organic anion/cation transporter), member 12 [Homo sapiens]Other Aliases: HGNC:17989, OAT4L, RST, URAT1Other Designations: organic anion transporter 4-like; solute carrier family 22 member 12; urate anion exchanger 1; urate transporter 1Chromosome: 11; Location: 11q13.1GeneID: 116085 7: AQP6 aquaporin 6, kidney specific [Homo sapiens]Other Aliases: HGNC:639, AQP2LOther Designations: Aquaporin-6, kidney specific; aquaporin 2-like, kidney specific; aquaporin 6Chromosome: 12; Location: 12q13GeneID: 363 8: SLC22A2 solute carrier family 22 (organic cation transporter), member 2 [Homo sapiens]Other Aliases: HGNC:10966, OCT2Other Designations: organic cation transporter 2; solute carrier family 22 member 2Chromosome: 6; Location: 6q26GeneID: 6582 9: SLC22A8 solute carrier family 22 (organic anion transporter), member 8 [Homo sapiens]Other Aliases: HGNC:10972, MGC24086, OAT3Other Designations: organic anion transporter 3; solute carrier family 22 member 8Chromosome: 11; Location: 11q11GeneID: 9376 10: SLC22A1 solute carrier family 22 (organic cation transporter), member 1 [Homo sapiens]Other Aliases: HGNC:10963, HOCT1, OCT1Other Designations: organic cation transporter 1; solute carrier family 22 member 1Chromosome: 6; Location: 6q26GeneID: 6580 11: SLC22A11 solute carrier family 22 (organic anion/cation transporter), member 11 [Homo sapiens]Other Aliases: HGNC:18120, MGC34282, OAT4, hOAT4Other Designations: organic anion transporter 4; solute carrier family 22 member 11Chromosome: 11; Location: 11q13.1GeneID: 55867 12: SLC22A4 solute carrier family 22 (organic cation transporter), member 4 [Homo sapiens]Other Aliases: HGNC:10968, MGC34546, OCTN1Other Designations: integral membrane transport protein; organic cation transporter 4; solute carrier family 22 member 4Chromosome: 5; Location: 5q23.3GeneID: 6583 13: SLC22A18 solute carrier family 22 (organic cation transporter), member 18 [Homo sapiens]Other Aliases: HGNC:10964, BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A1L, TSSC5, p45-BWR1AOther Designations: Beckwith-Wiedemann syndrome chromosome region 1, candidate A; efflux transporter-like protein; imprinted multi-membrane spanning polyspecific transporter-related protein; organic cation transporter-like 2; p45 Beckwith-Wiedemann region 1A; solute carrier family 22 (organic cation transporter), member 1-like; tumor suppressing subtransferable candidate 5; tumor-suppressing STF cDNA 5Chromosome: 11; Location: 11p15.5GeneID: 5002 14: SLC26A6 solute carrier family 26, member 6 [Homo sapiens]Other Aliases: HGNC:14472, DKFZp586E1422Other Designations: anion transporter 1; pendrin L1; pendrin-like protein 1; sulfate anion transporterChromosome: 3; Location: 3p21.3GeneID: 65010 15: SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2 [Homo sapiens]Other Aliases: HGNC:11006, GLUT2Chromosome: 3; Location: 3q26.1-q26.2GeneID: 6514 16: SLC29A2 solute carrier family 29 (nucleoside transporters), member 2 [Homo sapiens]Other Aliases: HGNC:11004, DER12, ENT2, HNP36Other Designations: equilibrative nucleoside transporter 2; hydrophobic nucleolar protein, 36kDChromosome: 11; Location: 11q13GeneID: 3177 17: SLC12A7 solute carrier family 12 (potassium/chloride transporters), member 7 [Homo sapiens]Other Aliases: HGNC:10915, DKFZP434F076, KCC4Other Designations: potassium/chloride transporter KCC4Chromosome: 5; Location: 5p15GeneID: 10723 18: SLC19A1 solute carrier family 19 (folate transporter), member 1 [Homo sapiens]Other Aliases: HGNC:10937, CHMD, FOLT, IFC1, REFC, RFC1Other Designations: Reduced Folate Carrier; homologue of mutant Chinese hamster cell methotrexate uptake deficiency; human reduced folate carrier (RFC); solute carrier family 19 member 1Chromosome: 21; Location: 21q22.3GeneID: 6573 19: SLC3A1 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1 [Homo sapiens]Other Aliases: HGNC:11025, ATR1, CSNU1, D2H, NBAT, RBATOther Designations: amino acid transporter 1; solute carrier family 3 (cystine, dibasic and neutral amino acid transporters), member 1; solute carrier family 3, member 1Chromosome: 2; Location: 2p16.3GeneID: 6519 20: ABCC4 ATP-binding cassette, sub-family C (CFTR/MRP), member 4 [Homo sapiens]Other Aliases: HGNC:55, EST170205, MOAT-B, MOATB, MRP4Other Designations: ATP-binding cassette, sub-family C, member 4; canalicular multispecific organic anion transporter (ABC superfamily)Chromosome: 13; Location: 13q32GeneID: 10257 21: SLCO4C1 solute carrier organic anion transporter family, member 4C1 [Homo sapiens]Other Aliases: HGNC:23612, OATP-H, OATP-M1, OATP4C1, OATPX, PRO2176, SLC21A20Chromosome: 5; Location: 5q21.2GeneID: 353189 22: SLC27A2 solute carrier family 27 (fatty acid transporter), member 2 [Homo sapiens]Other Aliases: HGNC:10996, FACVL1, FATP2, HsT17226, VLACS, VLCS, hFACVL1Other Designations: very long-chain fatty-acid-coenzyme A ligase 1; very-long-chain acyl-CoA synthetaseChromosome: 15; Location: 15q21.2GeneID: 11001 23: FCGRT Fc fragment of IgG, receptor, transporter, alpha [Homo sapiens]Other Aliases: HGNC:3621, FCRNChromosome: 19; Location: 19q13.3GeneID: 2217 24: SLC26A7 solute carrier family 26, member 7 [Homo sapiens]Other Aliases: HGNC:14467, SUT2Other Designations: sulfate anion transporterChromosome: 8; Location: 8q23GeneID: 115111 25: ABCC11 ATP-binding cassette, sub-family C (CFTR/MRP), member 11 [Homo sapiens]Other Aliases: HGNC:14639, MRP8Other Designations: ATP-binding cassette protein C11; ATP-binding cassette transporter MRP8; ATP-binding cassette, sub-family C, member 11; multi-resistance protein 8Chromosome: 16; Location: 16q12.1GeneID: 85320 26: ASPH aspartate beta-hydroxylase [Homo sapiens]Other Aliases: HGNC:757, BAH, CASQ2BP1, HAAH, JCTNOther Designations: aspartyl/asparaginyl-beta-hydroxylase; humbug; junctate; junctin isoform 1; peptide-aspartate beta-dioxygenaseChromosome: 8; Location: 8q12.1GeneID: 444 27: SLC4A1 solute carrier family 4, anion exchanger, member 1 (erythrocyte membrane protein band 3, Diego blood group) [Homo sapiens]Other Aliases: HGNC:11027, AE1, BND3, CD233, DI, EMPB3, EPB3, RTA1A, WD, WD1Other Designations: Waldner blood group; anion exchange protein 1Chromosome: 17; Location: 17q21-q22GeneID: 6521 28: SLC29A1 solute carrier family 29 (nucleoside transporters), member 1 [Homo sapiens]Other Aliases: HGNC:11003, ENT1Chromosome: 6; Location: 6p21.1-p21.2GeneID: 2030 29: NOS3 nitric oxide synthase 3 (endothelial cell) [Homo sapiens]Other Aliases: HGNC:7876, ECNOS, eNOSChromosome: 7; Location: 7q36GeneID: 4846 30: NOX4 NADPH oxidase 4 [Homo sapiens]Other Aliases: HGNC:7891, KOX, KOX-1, RENOXChromosome: 11; Location: 11q14.2-q21GeneID: 50507 31: HAAO 3-hydroxyanthranilate 3,4-dioxygenase [Homo sapiens]Other Aliases: HGNC:4796, 3-HAO, HAOChromosome: 2; Location: 2p21GeneID: 23498 32: DAO D-amino-acid oxidase [Homo sapiens]Other Aliases: HGNC:2671, DAAO, DAMOX, MGC35381, OXDAChromosome: 12; Location: 12q24GeneID: 1610 33: AQP2 aquaporin 2 (collecting duct) [Homo sapiens]Other Aliases: HGNC:634, AQP-CD, MGC34501, WCH-CDOther Designations: aquaporin 2; aquaporin-CD; collecting duct water channel proteinChromosome: 12; Location: 12q12-q13GeneID: 359 34: CUBN cubilin (intrinsic factor-cobalamin receptor) [Homo sapiens]Other Aliases: HGNC:2548, IFCR, MGA1, gp280Other Designations: cubilin; intrinsic factor B12-receptor; intrinsic factor-cobalamin receptorChromosome: 10; Location: 10p12.31GeneID: 8029 35: UCP2 uncoupling protein 2 (mitochondrial, proton carrier) [Homo sapiens]Other Aliases: HGNC:12518, SLC25A8, UCPHOther Designations: Uncoupling protein-2; uncoupling protein 2Chromosome: 11; Location: 11q13GeneID: 7351 36: RBP1 retinol binding protein 1, cellular [Homo sapiens]Other Aliases: HGNC:9919, CRABP-I, CRBP, CRBP1, RBPCOther Designations: retinol-binding protein 1, cellularChromosome: 3; Location: 3q23GeneID: 5947 37: GRIA4 glutamate receptor, ionotrophic, AMPA 4 [Homo sapiens]Other Aliases: HGNC:4574, GLUR4, GLUR4C, GLURDOther Designations: glutamate receptor, ionotrophic; glutamate receptor, ionotropic, AMPA 4Chromosome: 11; Location: 11q22GeneID: 2893 38: SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip) [Homo sapiens]Other Aliases: HGNC:10681, IP, SDH, SDH1, SDHIPOther Designations: iron-sulfur subunitChromosome: 1; Location: 1p36.1-p35GeneID: 6390 39: PTGDS prostaglandin D2 synthase 21kDa (brain) [Homo sapiens]Other Aliases: HGNC:9592, PDS, PGD2, PGDS, PGDS2Other Designations: PGD2 synthase; beta-trace protein; glutathione-independent PGD synthase; lipocalin-type prostaglandin D synthase; prostaglandin D synthase; prostaglandin D2 synthase (21kD, brain); prostaglandin D2 synthase 21kDa; prostaglandin-H2 D-isomeraseChromosome: 9; Location: 9q34.2-q34.3GeneID: 5730 40: NOS1 nitric oxide synthase 1 (neuronal) [Homo sapiens]Other Aliases: HGNC:7872, NOSChromosome: 12; Location: 12q24.2-q24.31GeneID: 4842 41: ATP1A2 ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide [Homo sapiens]Other Aliases: HGNC:800, FHM2, MGC59864, MHP2Other Designations: Na+/K+ -ATPase alpha 2 subunit proprotein; Na+/K+ ATPase 2; Na+/K+ ATPase, alpha-A(+) catalytic polypeptide; Na+/K+ ATPase, alpha-B polypeptide; migraine, hemiplegic 2; sodium pump 2; sodium-potassium ATPase; sodium/potassium-transporting ATPase alpha-2 chainChromosome: 1; Location: 1q21-q23GeneID: 477 42: AQP3 aquaporin 3 [Homo sapiens]Other Aliases: HGNC:636Chromosome: 9; Location: 9p13GeneID: 360 43: APOE apolipoprotein E [Homo sapiens]Other Aliases: HGNC:613, AD2, MGC1571Other Designations: Alzheimer disease 2 (APOE*E4-associated, late onset); apolipoprotein E precursor; apolipoprotein E3Chromosome: 19; Location: 19q13.2GeneID: 348 44: WT1 Wilms tumor 1 [Homo sapiens]Other Aliases: HGNC:12796, GUD, WAGR, WIT-2, WT33Chromosome: 11; Location: 11p13GeneID: 7490 45: SGK serum/glucocorticoid regulated kinase [Homo sapiens]Other Aliases: HGNC:10810, SGK1Other Designations: serine/threonine protein kinase SGKChromosome: 6; Location: 6q23GeneID: 6446 46: IGF1 insulin-like growth factor 1 (somatomedin C) [Homo sapiens]Other Aliases: HGNC:5464, IGFIOther Designations: insulin-like growth factor 1 (somatomedia C)Chromosome: 12; Location: 12q22-q23GeneID: 3479 47: IGF2 insulin-like growth factor 2 (somatomedin A) [Homo sapiens]Other Aliases: HGNC:5466Other Designations: insulin-like growth factor 2; somatomedin AChromosome: 11; Location: 11p15.5GeneID: 3481